Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108581011G>ACA258356COL4A5c.920G>A (p.Gly307Asp)
c.596G>A (p.Gly199Asp)
c.935G>A (p.Gly312Asp)
 ClinVar dbSNP COSMIC
Xg.108581011G=CA2450683197COL4A5c.920G= (p.Gly307=)
c.596G= (p.Gly199=)
c.935G= (p.Gly312=)
 dbSNP

Number of alleles fetched